Canonical Allele Identifier: PA2827959030
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230530
ClinVar RCV Id: RCV004520681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln1539Leu
CA16031374
NM_001354897.2:c.4616A>T